MUTANT PYRROLYSYL -tRNA SYNTHETASE, AND METHOD FOR PRODUCTION OF PROTEIN HAVING NON-NATURAL AMINO ACID INTEGRATED THEREIN BY USING THE SAME

ABSTRACT

Method for incorporating a lysine derivative (particularly an N ε -benzyloxycarbonyl-lysine (Z-Lys) derivative) having useful functional group such as heavy atom, selenium, reactive functional group, fluorescent group or crosslinker, which is suitable as a non-natural amino acid, into a desired protein in a site-specific manner. A mutant pyrrolysyl-tRNA synthetase has substitution of at least one amino acid residue selected from tyrosine residue at position 306, leucine residue at position 309 and cysteine residue at position 348 each constituting a pyrrolysine-binding site in the amino acid sequence for pyrrolysyl-tRNA synthetase of SEQ ID NO:2. The substitution of the amino acid residue is: of tyrosine residue at position 306 by glycine or alanine residue, of leucine residue at position 309 by glycine or alanine residue, and/or of a cysteine residue at position 348 by valine, serine or alanine residue.

REFERENCE TO RELATED APPLICATION

This application is a Divisional of application Ser. No. 12/727,037,filed Mar. 18, 2010, which is a Continuation of PCT InternationalApplication No. PCT/JP2008/067029 filed on Sep. 19, 2008, and whichclaims priority to Patent Application No. 2007-243574, filed in Japan onSep. 20, 2007. The entire contents of all of the above applications arehereby incorporated by reference.

TECHNICAL FIELD

This application is based upon and claims the benefit of the priority ofJapanese patent application No. 2007-243574, filed on Sep. 20, 2007, thedisclosure of which is incorporated herein in its entirety by referencethereto.

The present invention relates to a mutant pyrrolysyl-tRNA synthetase,and a method for production of a protein having non-natural amino acidintegrated therein by using the same. In further detail, the presentinvention relates to a method for site-specific incorporation of anN^(ε)-benzyloxycarbonyl-lysine derivative into a protein of interestusing Methanosarcina-derived mutant pyrrolysyl-tRNA synthetase andsuppresser tRNA.

BACKGROUND ART

A non-natural amino acid-incorporated protein (alloprotein) which has asubstitution of an amino acid residue at a desired position by an aminoacid (a non-natural amino acid) other than 20 kinds of amino acidsinvolved in normal protein synthesis could be an effective measure ofanalyzing the structure and function of a protein. Over 30 kinds ofalloproteins have already been synthesized using aminoacyl-tRNAsynthetase (aaRS)/tRNA pair derived from various biological species. Asystem which has most long history and is applied to incorporation of alot of useful non-natural amino acids is a pair of a tyrosyl-tRNAsynthetase (TyrRS) mutant and an amber-suppressed tRNA^(Tyr). In thismethod, the following orthogonal relationship makes a key point: each ofaaRSs in two groups of eubacteria and of archaebacteria and eukaryotesmay aminoacylate tRNA in its group, whereas it could not aminoacylatetRNAs in the other group. For example, the TyrRS/tRNA^(Tyr) pair ofarchaebacterium Methanocaldococcus jannaschii is an orthogonal pair inE. coli system, whereas the pair of Escherichia coli TyrRS and Bacillusstearothermophilus tRNA^(Tyr) is an orthogonal pair in mammalian cellsystem. Therefore, these pairs may be used for extending genetic code intheir systems (see, for example, Patent Document 1 and Non-PatentDocument 1).

On the other hand, Methanosarcina mazei-derived pyrrolysyl-tRNAsynthetase (PylRS) and amber suppressor tRNA^(Pyl) function asorthogonal aaRS/tRNA pair in E. coli cells (see, for example, Non-PatentDocument 2). Furthermore, it is reported that this pair may also be usedfor extending genetic code in eukaryotic cell (see, for example, PatentDocument 2). Pyrrolysine is a lysine derivative having a bulkymethylpyrroline moiety at the side chain. Wild-type PylRS may bindN^(ε)-Boc-L-Lysine to tRNA^(Pyl) in E. coli cells (see Patent Document2). Moreover, X-ray crystal structure of a complex of wild-type PylRS,ATP analog, and pyrrolysine or pyrrolysine analog is reported (seeNon-Patent Documents 3, 4 and 9).

-   [Patent Document 1] WO2004/070024-   [Patent Document 2] Japanese Patent Kokai Publication No.    JP-P2007-37445A-   [Non-Patent Document 1] Sakamoto, K. et al., Nucleic Acids Research,    2002, Vol. 30, pp. 4692-4699.-   [Non-Patent Document 2] Blight S. K. et al., Nature, (2004) Vol.    431, pp. 333-335.-   [Non-Patent Document 3] Yanagisawa, T. et al., Acta Cryst. (2006)    F62, 1031-1033-   [Non-Patent Document 4] Kavran, J. M. et al., Proc. Natl. Acad.    Sci. (2007) Vol. 104, pp. 11268-11273-   [Non-Patent Document 5] Tsao, M.-L., Tian, F., Schultz, P. G.    ChemBioChem Vol. 2005, Issue 6, pp. 2147-2149-   [Non-Patent Document 6] Ohno, S. et al., J. Biochem. (Tokyo) Vol.    141, pp. 335-343 (2007)-   [Non-Patent Document 7] Mukai, et al., Biochem. Biophys. Res.    Commun. Vol. 371, pp. 818-822 (2008)-   [Non-Patent Document 8] Liu, W. et al., Nat. Methods. Vol. 4, pp.    239-244 (2007)-   [Non-Patent Document 9] Yanagisawa, T. et al., J. Mol. Biol. (2008)    378, 634-652

SUMMARY

The entire disclosures of Patent Documents 1 and 2, and Non-PatentDocuments 1-9 as mentioned above are incorporated herein by referencethereto. An analysis of related technology according to the presentinvention is given below.

A method for incorporating a tyrosine analog into a desired position ofa protein using TyrRS/tRNA^(Tyr) system is useful as a method forincorporating an amino acid containing a heavy atom for the phasedetermination due to the strict structure of a tyrosine analog with anaromatic ring. On the other hand, structural flexibility of anon-natural amino acid to be incorporated is required for incorporatinga reactive amino acid with cross-linker, triple bond, double bond andthe like into a protein and searching a target interacting with thisprotein in the cell. Therefore, it is thought that a lysine derivativehaving more flexible structure of its amino acid side chain is superiorto a tyrosine analog. Generally, in order to modify the substratespecificity of lysyl-tRNA synthetase (LysRS), a method for incorporatinga lysine derivative into a protein is used. However, LysRS has strictrecognition of lysine so that, up to now, it is difficult tosite-specifically incorporate a lysine derivative with a functionalgroup of various sizes and forms into a protein. The present inventionis aimed at providing a method for site-specifically incorporating intodesired protein a lysine derivative, particularly anN^(ε)-benzyloxycarbonyl-lysine (Z-Lys) derivative, which is suitable asa non-natural amino acid having a useful functional group such as aheavy atom, selenium, a reactive functional group, a fluorescent group,a crosslinker and the like.

The present invention is provided for solving the problem as mentionedabove. The inventors found that a Methanosarcina-derived pyrrolysyl-tRNAsynthetase is a unique aaRS which has low amino acid substratespecificity and is capable of activating not only pyrrolysine but alsolysine derivatives with various hydrophobic functional groups.Furthermore, the inventors found a PylRS mutant capable of efficientlyaminoacylating a Z-Lys derivative with bulky side chain structure. Thepresent invention is completed on the basis of those findings.

That is, in a first aspect, the present invention provides a mutantpyrrolysyl-tRNA synthetase comprising a substitution of at least oneamino acid residue selected from tyrosine at position 306, leucine atposition 309, and cysteine at position 348, which constitute apyrrolysine-binding site, in the amino acid sequence of thepyrrolysyl-tRNA synthetase set forth in SEQ ID NO:2. The substitution ofthe amino acid residue is: substitution of tyrosine at position 306 byglycine or alanine, substitution of leucine at position 309 by glycineor alanine, and/or substitution of cysteine at position 348 by valine,serine or alanine. In a preferable embodiment, the mutantpyrrolysyl-tRNA synthetase further comprises amino acid substitution oftyrosine at position 384 by phenylalanine or histidine.

In one preferable embodiment of the present invention, a mutantpyrrolysyl-tRNA synthetase is provided whose amino acid sequencecomprises one or several amino acid deletion(s), substitution(s), oraddition(s) at position(s) other than at positions 306, 309, 348 and384, and which is capable of aminoacylatingN^(ε)-benzyloxycarbonyl-lysine. In a further different embodiment, amutant pyrrolysyl-tRNA synthetase is provided which is obtained from awild-type pyrrolysyl-tRNA synthetase, which is Methanosarcina-derivedpyrrolysyl-tRNA synthetase that is a homolog of the amino acid sequenceset forth in SEQ ID NO:2, so substituted that when the amino acidsequence of said homolog is aligned with the amino acid sequence setforth in SEQ ID NO:2, the homolog has substitution of alanine fortyrosine corresponding to position 306 of the amino acid sequence setforth in SEQ ID NO:2 and/or substitution of phenylalanine for tyrosinecorresponding to position 384 thereof.

In another (second) aspect, the present invention provides an isolatedDNA encoding the mutant pyrrolysyl-tRNA synthetase as well as anexpression vector and a transformant containing the DNA, and the like.

In a further different (third) aspect, the present invention provides amethod of producing a non-natural amino acid-incorporated proteinwherein the following (a) to (c) are expressed in a cell or cell extractin the presence of an N^(ε)-benzyloxycarbonyl-lysine derivative: (a) anaminoacyl-tRNA synthetase capable of activating theN^(ε)-benzyloxycarbonyl-lysine derivative; (b) a suppressor tRNA capableof binding to the N^(ε)-benzyloxycarbonyl-lysine derivative in thepresence of said aminoacyl-tRNA synthetase, and (c) a gene encoding adesired protein that has nonsense mutation or frameshift mutation at adesired position. It is preferred that theN^(ε)-benzyloxycarbonyl-lysine derivative isNE-ortho-iodo-benzyloxycarbonyl-lysine;benzyloxycarbonyl-aminoethyl-selenocysteine;N^(ε)-ortho-ethinyl-benzyloxycarbonyl-lysine;N^(ε)-ortho-azide-benzyloxycarbonyl-lysine; orN^(ε)-ortho-diaziryl-benzyloxycarbonyl-lysine.

In a furthermore different (fourth) aspect, the present inventionprovides a kit for synthesizing non-natural amino acid-incorporatedprotein comprising (a) cell extract; (b) a non-natural amino acidcomprising N^(ε)-benzyloxycarbonyl-lysine derivative; (c) the mutantpyrrolysyl-tRNA synthetase of the present invention; and (d) asuppressor tRNA capable of binding to an N^(ε)-benzyloxycarbonyl-lysinederivative in the presence of said mutant pyrrolysyl-tRNA synthetase.

The PylRS mutant of the present invention has enhanced activity againstZ-Lys with bulky side chain structure and derivatives thereof.Accordingly, it is possible to site-specifically incorporate a Z-Lysderivative efficiently into a desired protein in endogenous proteinsynthetic system of E. coli, animal cells and the like.

BRIEF DESCRIPTION OF THE DRAWINGS

In FIG. 1, (A) shows chemical structure of L-pyrrolysine; (B) showsdomain structure of M. mazei-derived PylRS; (C) shows a result obtainedfrom detection of pyrrolysine binding reaction to tRNA^(Pyl) using PAGEand methylene blue staining; and (D) shows overall structure of PylRS(c270).

FIGS. 2A and 2B shows tertiary structure-based sequence alignmentsbetween M. mazei PylRS (c270) and other PylRS and LysRS (SEQ ID NOS:9-16).

FIG. 3A shows comparison between an active site of PylRS (c270) (see.FIG. 3C) and an active site of LysRS (see FIG. 3D).

FIG. 3B shows a result obtained from research of effect of mutationincorporated at the active site of PylRS (c270) on aminoacylationreaction of pyrrolysine.

FIG. 3C shows a close-up view of the active site in PylRS (c270).

FIG. 3D shows a close-up view of the active site in LysRS.

FIG. 3E shows comparison between an active site of PylRS (c270) (see.FIG. 3F) and an active site of LysRS (see FIG. 3D) in the case ofpyrrolysine being an axial-type stereoisomer.

FIG. 3F shows a close-up view of the active site in PylRS (c270) in thecase of pyrrolysine being an axial type stereoisomer.

In FIG. 4, (A) shows chemical structures of the lysine derivatives; and(B) shows results obtained from analysis of aminoacylation reaction ofthese derivatives using acidic urea PAGE.

In FIG. 5, (A) and (B) show modes of Z-Lys binding to PylRS(c270) andPylRS(c270) (Y306A) active sites; and (C) shows results obtained fromanalysis of aminoacylation reaction of Z-Lys with various types of PylRSmutants.

FIG. 6 shows outline of amber suppression system using PylRS andtRNA^(Pyl).

FIG. 7 shows results obtained from SDS-PAGE analysis of proteins whichwere synthesized by Boc-Lys and Aloc-Lys dependent amber suppression inE. coli.

FIG. 8 shows results obtained from SDS-PAGE analysis of proteins whichwere synthesized by Z-Lys dependent amber suppression in E. coli.

FIG. 9 shows results obtained from analysis of purified GST proteinswhich were synthesized by amber suppression in E. coli.

FIG. 10 shows results obtained from analysis by MALDI-TOF massspectrometry of purified GST proteins (SEQ ID NOS: 17 and 18) which weresubjected to in-gel trypsin digestion.

FIG. 11A shows putative secondary structure of M. mazei tRNA^(Pyl) (SEQID NO: 3).

FIG. 11B shows results obtained from research of aminoacylation activityfor a variety of nonsense codons.

FIG. 12A-12E shows schematic views of chemical structures of a varietyof N^(ε)-benzyloxycarbonyl-lysine derivatives and their binding modeswith PylRS (Y306A).

FIG. 13 shows results obtained from SDS-PAGE analysis of GST havingamber codon which is expressed in E. coli using mutant enzyme havinghigh Z-Lys specificity.

FIG. 14 shows patterns resulting from separating, using SDS-PAGE, crudeextracts obtained from E. coli in which GST amber gene was expressed andthen staining the proteins.

FIG. 15 shows chemical structure of FITC-PP3.

FIG. 16 shows results obtained from SDS-PAGE separation of GSTs whichare subjected to 2 types of fluorescence modification reactions and thendetection of fluorescence using UV light.

FIG. 17 shows results (or levels) of expression of LacZ protein fromlacZ amber gene, which are shown in relative intensity of coloringreaction.

FIG. 18 shows results obtained by performing fluorescence modificationreaction in crude extract form animal cells in which Grb2 gene wasexpressed, and conducting SDS-PAGE separation, and then implementingdetection using fluorescence detector.

PREFERRED MODES [Pyrrolysyl-tRNA Synthetase (PylRS)]

Pyrrolysyl-tRNA synthetase (PylRS) of the present invention may beproduced by mutagenesis, in various methods, of wild-type PylRS obtainedfrom archaebacteria, particularly form methanogenic archaebacteria.Wild-type PylRS may be obtained from, but not restricted to, forexample, Methanosarcina mazei (M. mazei), Methanosarcina barkeri (M.barkeri) and Methanosarcina acetivorans (M. acetivorans) and the like,which are methanogenic archaebacteria. Genomic DNA sequences of a lot ofbacteria including those archaebacteria and amino acid sequences basedon these nucleic acid sequences are known and it is also possible toobtain another homologous PylRS from public database such as GenBank byperforming homology search for the nucleic acid sequences and the aminoacid sequences, for example. M. mazei-derived PylRS, as typicalexamples, is deposited as Accession No. AAM31141, M. barkeri-derivedPylRS is deposited as Accession No. AAL40867 and M. acetivorans-derivedPylRS is deposited as accession No. AAM03608. M. mazei-derived PylRS asmentioned above is particularly preferred, the nucleic acid sequence ofwhose gene is shown in SEQ ID NO:1, and the amino acid sequence of whoseprotein is shown in SEQ ID NO:2. Sequences of PylRS homologs of theMethanosarcina are well conserved. For example, homology in amino acidsequences of the homologs is approximately 70% or more. Tertiarystructures of these wild-type PylRSs are analyzed, and according to themethod detailed below, PylRS mutants of the present invention areproduced.

[Production of PylRS Mutants]

The present invention provides PylRS mutants which are produced on thebasis of analysis of tertiary structure of catalytic domain in PylRS anda method for random mutagenesis. Concrete methods for crystallization ofa complex of PylRS, substrate amino acids (pyrrolysine or Boc-Lys) andAMPPNP, which is an ATP analog, and for analysis of X-ray structurethereof are described below in Examples. As unit cell parameters of acrystal complex of M. mazei-derived PylRS catalytic domain, pyrrolysineand AMPPNP, space group is P6₄, unit cell is a=b=104.88 angstrom,c=70.43 angstrom, alpha=beta=90 degrees and lambda=120 degrees. Here,“unit cell” means a smallest and simple volume factor of crystal, and“space group” means symmetry of a unit cell. Methods for crystallizationof catalytic domain of PylRS and for analysis of X-ray structure thereofhave been already reported by the present inventors (see Non-PatentDocument 3 as cited above, the entity of which is incorporated herein byreference).

For recognition of amino acid substrate by PylRS, it is important that alysine derivative has a carbonyl which binds to its epsilon amino groupand a hydrophobic functional group added to the end of the carbonyl.Wild-type PylRS may activate lysine derivatives in a case where thelysine derivatives have a hydrophobic functional group such as a pyrrolering which has a certain degree of size and bulkiness. However, there isa limit to the size of lysine derivatives which can be activated bywild-type PylRS. For example, a lysine derivative with a largefunctional group, such as N^(ε)-benzyloxycarbonyl-lysine (Z-Lys), cannotbe incorporated into a protein. According to the PylRS mutant of thepresent invention, it is possible to incorporate Z-Lys, which is merelyweakly activated by wild-type PylRS, into a protein efficiently.

Those PylRS mutants include a PylRS mutant comprising a substitution ofat least one amino acid residue selected from tyrosine at position 306,leucine at position 309, and cysteine at position 348, which constitutea pyrrolysine binding site, in the amino acid sequence set forth in SEQID NO:2. Such amino acid substitution is preferably substitution oftyrosine at position 306 in SEQ ID NO:2 by an amino acid residue withcomparatively small side chain structure, such as glycine, alanine,serine and threonine, more preferably substitution by glycine oralanine, most preferably substitution by alanine. Because an amino acidresidue at position 306 in PylRS constitutes a substrate-binding site,it is thought to be preferable that the amino acid residue at position306 is replaced with the above mentioned amino acid residues in order toavoid steric hindrance to binding of a substrate, particularly in a casewhere the substrate has a bulky side chain such as a Z group.Furthermore, leucine residue at position 309 may be replaced withglycine or alanine, preferably with alanine. In this case, it ispreferable that cysteine at position 348 is also replaced with valine oralanine.

Further, it is preferable that tyrosine at position 384 in SEQ ID NO:2is replaced with phenylalanine, valine, leucine, isoleucine, histidineand the like, more preferably with phenylalanine or histidine, mostpreferably with phenylalanine. In addition, glycine at position 131 maybe replaced with glutamic acid. Although the effect of the above aminoacid substitution on enhancement of activity is not necessarily evident,it is demonstrated that an amino acid residue at position 384 interactswith a substrate amino acid, particularly with the main chain partthereof (see Non-Patent Document 4). Therefore, there is likelihood thatcatalytic activity is enhanced independently of types of the substrateamino acid. Preferably this amino acid substitution at position 384coexists with amino acid substitution at the above mentionedsubstrate-binding site, more preferably with amino acid substitution atposition 306 or 309 as a double mutant, or with amino acid substitutionat position 309 and 348 as a triple mutant.

In a preferable embodiment, the present invention provides a mutantPylRS comprising substitution of tyrosine residues at positions 306 and384 by alanine and phenylalanine residues, respectively, in the aminoacid sequence set forth in SEQ ID NO:2. This mutant PylRS (Y306A, Y384F)can efficiently aminoacylate a lysine derivative with bulky side chainstructure such as Z-Lys. Herein, “being capable of aminoacylating” or“aminoacylation activity” means an activity for binding a lysinederivative to suppressor tRNA to synthesize aminoacyl tRNA. For example,it is possible to determine the amount of pyrrolysyl-tRNA (Pyl-tRNA)which is produced by purifying mutant enzyme and suppressor tRNA, andperforming in vitro enzymatic reaction in the presence of ATP and alysine derivative.

Usable methods for producing those mutants may include a variety ofmethods which are known to a person skilled in the art. For example, itis possible that using a primer that has substitution of nucleic acidsequence encoding the position of an amino acid of interest by nucleicacid sequence encoding an amino acid to be altered, a DNA that hassubstitution by nucleic acid sequence encoding the amino acid to bealtered is amplified by PCR to obtain a DNA encoding a full lengthmutant PylRS, and the DNA is expressed using host cells such as E. colicells. Alternatively, production of the mutants may be performed byknown methods for site-specific mutagenesis, such as Kunkel method andGapped duplex method. It is possible to use a kit for mutagenesis usingthese procedures (for example, Mutan-K, Mutan-G (TAKARA) and the like).

Further, the present invention includes a protein comprising amino acidsequence which has one or several amino acid deletions, substitutions,insertions or additions at positions other than at positions 306, 309,348 and 384 in the amino acid sequence of the above-mentioned mutantPylRS, and which is capable of aminoacylating Z-Lys. “One or severalamino acids” means approximately at most 5-10% of full length amino acidresidues, for example, approximately 1-50 residues, preferably 1-20residues, more preferably 1-10 residues, most preferably 1-5 residues.Likewise, the mutant PylRS of the present invention may havepredetermined mutations at positions 306, 309, 348 and 384 in theabove-mentioned amino acid sequence. As to the other amino acidresidues, the mutant PylRS of the present invention may be of 70% ormore homology, preferably of 80% or more homology, more preferably of90% or more homology, as long as it maintains desired activity.

[Non-Natural Amino Acid]

As a non-natural amino acid used herein, for example,N^(ε)-benzyloxycarbonyl-lysine (Z-Lys) derivative may be used. Z-Lysderivative is non-natural amino acid, and is suitably used as an aminoacid which has reactive backbone having high flexibility comparing tothose of tyrosine analog because the alkyl moiety in lysine side chainthereof serves as a linker. The Z group is generally known as aprotecting group for peptide synthesis. However, the Z group is of highvariability comparing to benzoyl (Bz) group and is of comparably highwater solubility due to oxygen contained in its side chain. As a result,the Z group is easy to handle in aqueous conditions. In addition, sincethe Z group may be deprotected by catalytic hydrogen reduction which isa mild condition, it is possible that proteins which are linked with acrosslinker type Z-Lys derivative are separated in stable condition, andthat a fluorescence probe etc. which is bound to a protein via thereactive functional group is, as necessary, cut off from the protein.

On the basis of binding models of Z-Lys to active sites in wild-typePylRS and mutant PylRS (Y306A), some preferable compounds may beobtained. It is expectable that ortho-position on the benzene ring ofthe Z group faces toward outside of the active site and thus does noteasily cause steric hindrance. Therefore, substitution of a functionalgroup which has comparative large size can be conducted. For example,Z-Lys derivatives with a crosslinker (azide, diazirine), a reactivefunctional group (alkyne) at the ortho-position, Z-Lys derivative withan atom for structural analysis phase determination (selenium) at thealkyl side chain etc. may be exemplified. In addition, the following areexemplified as Z-Lys derivative which may match with thesubstrate-binding site of PylRS mutant (Y306A):N^(ε)-ortho-iodo-benzyloxycarbonyl-lysine,benzyloxycarbonyl-aminoethyl-selenocysteine,N^(ε)-ortho-ethinyl-benzyloxycarbonyl-lysine,N^(ε)-ortho-azide-benzyloxycarbonyl-lysine andN^(ε)-ortho-diaziryl-benzyloxycarbonyl-lysine (see FIG. 12)

[Suppressor tRNA]

It is required that tRNA which is used in combination with theabove-mentioned pyrrolysyl-tRNA synthetase (PylRS) should meet thefollowing requirements that it is assigned to a nonsense codon otherthan codons assigned to natural amino acids of 20 kinds, and that it isrecognized merely by the above-mentioned mutant PylRS but is notrecognized by normal aminoacyl-tRNA synthetase in host (orthogonaltRNA), and should be expressed in eubacteria or mammalian cells. As suchtype of tRNA, archaea-derived suppressor tRNA is exemplified.

Here, as nonsense codons, UAG (amber), UAA (ochre), UGA (opal) areexemplified, it is preferable that UAG (amber) or UGA (opal) are used.As an alternative to the nonsense codons, a codon consisting of 4 ormore bases (preferably 4 or 5 bases) (hereinafter referred to as“frameshift codon”) may be used.

Those tRNAs may be prepared by, for example, obtaining a genecorresponding to tRNA^(Pyl) from the above-mentioned archaebacteriagenome, and expressing in vitro or in vivo this gene directly or afterintroduction of desired mutation. As an example, M. mazei-derivedwild-type tRNA has the following nucleic acid sequence: tRNA^(Pyl):

(SEQ ID NO: 3) 5′-GGAAACCUGAUCAUGUAGAUCGAAUGGACUCUAAAUCCGUUCAGCCGGGUUAGAUUCCCGGGGUUUCCGCCA-3′.[DNA Encoding Mutant PylRS of the Present Invention, Expression VectorComprising this DNA, and Transformant]

The present invention includes DNA encoding mutant PylRS which isobtained by the above-mentioned manner. In a preferable embodiment, DNAof the present invention includes DNA comprising substitution of codons(TAC) and (TAT), which each correspond to tyrosine, at positions 306 and384 by codon (GCT, GCC, GCA or GCG), which corresponds to alanine, andcodon (TTT or TTC), which corresponds to phenylalanine, respectively, inthe DNA encoding wild-type PylRS set forth in SEQ ID NO:1. In addition,codon of an amino acid at position 306 may be a codon (GGT, GGC, GGA orGGG) corresponding to glycine, and a codon of an amino acid at position384 may be a codon (CAT or CAC) corresponding to histidine.

Further, the DNA of the present invention includes DNA which has atleast 80% or more, preferably 90% or more, further preferably 95% ormore homology with the DNA consisting of the nucleic acid sequence setforth in SEQ ID NO:1 in the case of calculation in default condition byBLAST and the like; and whose codons of the amino acid chain atpositions 306 and 384 are codons corresponding to alanine andphenylalanine, respectively. Furthermore, RNAs corresponding to theabove-mentioned DNA, for example, mRNA transcripted from the DNA orantisense RNA and the like, are also included in the present invention.

The DNA of the present invention also includes DNA which hybridizesunder stringent condition with DNA comprising sequence complementary tothe above-mentioned DNA and encodes mutant PylRS capable ofaminoacylating N^(ε)-benzyloxycarbonyl-lysine. Here, “hybridize understringent condition” is an experimental condition well-known to a personskilled in the art. Concretely, “stringent condition” is a conditionwhich allows identification in such a manner as to perform hybridizationin the presence of 0.7-1 M of NaCl at ca. 60-68 degrees Celsius,followed by washing at ca. 65-68 degrees Celsius using 0.1-2×SSCsolution (wherein “1×SSC” comprises 150 mM of NaCl and 1.15 mM of sodiumcitrate). For selecting stringency, in the washing step, saltconcentration and temperature may be optimized as necessary. Inaddition, it is a common technical knowledge of a person skilled in theart to add formamide, SDS and the like for increasing stringency.

The present invention also includes an expression vector capable ofexpressing mutant PylRS by link (insert) of the DNA of the presentinvention. A vector for insertion of the DNA of the present inventionincludes any vectors that may be replicated in hosts and includes, butis not particularly restricted to, plasmid DNA, bacteriophage DNA andthe like. In the expression vector of the present invention, preferably,the DNA of the present invention is integrated into the vector such thatwhen the vector is introduced into host cells, the above-mentionedmutant PylRS may be produced in the host cells. Accordingly, to thevector of the present invention may be linked DNA which contains, inaddition to promoters (for example, T7 promoter, CMV promoter, trppromoter, lac promoter, PL promoter, tac promoter and the like), ciselement such as enhancer, splicing signal, poly A attachment signal,selection marker, ribosome binding sequence (SD sequence) and the likeis linked, as necessary. As a selection marker, for example,dihydrofolate reductase gene, ampicillin resistance gene, neomycinresistance gene and the like are exemplified.

The present invention includes transformant, preferably eubacteria andeukaryotic cell, which was transformed with the expression vector of thepresent invention. Herein, “eubacteria” includes bacteria which belongto, for example, Escherichia such as Escherichia coli (E. coli),Bacillus such as Bacillus subtilis, Pseudomonas such as Pseudomonasputida, Rhizobium such as Rhizobium meliloti. Further, “eukaryotic cell”includes yeasts such as Saccharomyces cerevisiae and Schizosaccharomycespombe, and animal cells such as COS cell and CHO cell. Transformationmay be performed by a known method such as, for example, a method usingcalcium ion (Cohen, S. N. et al. (1972) Proc. Natl. Acad. Sci., USA 69,2110-2114), DEAE-dextran method, electroporation method and the like.

[Production of Z-Lys Derivative-Incorporated Protein]

Mutant PylRS thus obtained may be used for production of Z-Lysderivative-incorporated protein, in vitro or in vivo, in combinationwith suppressor tRNA derived from archaea or eukaryote. That is, thepresent invention provides a method of producing a Z-Lysderivative-incorporated protein including expressing (a) anaminoacyl-tRNA synthetase for the Z-Lys derivative, (b) a suppressortRNA capable of binding to the Z-Lys derivative in the presence of theaminoacyl-tRNA synthetase, and (c) a gene encoding a desired proteinthat has a nonsense mutation or frameshift mutation at a desiredposition in a cell or cell extract in the presence of the Z-Lysderivative. Here, a synthesis system for PylRS and suppressor tRNAincludes any expression system, and, for example, includes, but is notparticularly restricted to, cell-free protein synthesizing system,protein synthesizing system in cells of eubacteria, and eukaryoticcells, preferably animal cells, particularly preferably mammalian cells.

The cell-free protein synthesizing system is a system for synthesizing adesired protein by obtaining protein factors required for translation ofprotein as a form of cell extract, followed by reconstituting thisreaction in vitro. The cell-free system may be constituted usingextracts derived from various biological species. For example, thefollowing may be used: extracts of eukaryotic cells and prokaryotic cellunder conditions of high protein synthesizing activity, such as, forexample, bacteria such as E. coli and thermophilic bacterium, wheatgerm, rabbit reticulocyte, mouse L-Cell, Ehrlich ascites carcinoma cell,HeLa cell, CHO cell, and budding yeast (Clemens, M. J., Transcriptionand Translation—A Practical Approach, (1984), pp. 231-270, Henes, B. D.et al. eds., IRL Press, Oxford).

Usable extracts from E. coli may include S30 extract prepared by themethod disclosed in Zubay et al. (Ann. Rev. Genet. Vol. 7, pp. 267-287(1973)) or Pratt, J. M. et al., (Transcription and Translation—APractical Approach, (1984), pp. 179-209, Henes, B. D. et al. eds., IRLPress, Oxford)). E. coli S30 extract contains all enzymes and factors ofE. coli cells required for transcription and translation. Furthermore,supplemental liquid mixture may be added. In a concrete preparationmethod: first, E. coli cells are is cultured to collect the cells usingcentrifugation and the like; the collected cells are washed to bere-suspended in buffer, followed by destructing them using French press,glass beads, Waring blender and the like; insoluble substances ofdestructed E. coli cells are removed using centrifugation, followed bymixing the remainder with pre-incubation liquid mixture to be incubated,thereby endogenous DNA and RNA being degraded, in addition to whichendogenous nucleic acids may be degraded by adding calcium salt,nuclease from Micrococcus and the like; subsequently, endogenous aminoacids, nucleic acids, nucleosides and the like are removed usingdialysis, followed by aliquoated and stored in liquid nitrogen or at ca.−80 degrees Celsius.

In the case of performing reaction of synthesizing Z-Lysderivative-incorporated protein, the cell extracts as mentioned abovemay contain DNA or RNA which encodes a desired protein that has nonsensemutation or frameshift mutation at a desired position oftranscription/translation templates; amino acids which include Z-Lysderivative; mutant PylRS of the present invention; suppressor tRNA whichis capable of binding to Z-Lys derivative in the presence of the mutantPylRS; energy source; a variety of ions; buffer; ATP regeneratingsystem; nuclease inhibitor, tRNA, reducing agent; polyethylene glycol;cAMP; folates and antimicrobial agent, and, in cases where DNA is usedas template, the cell extracts as mentioned above may include furthersubstrate for RNA synthesis and RNA polymerase and the like. Theseelements are selected and prepared as required according to types ofproteins of interest and protein synthesizing systems to be used. Forexample, in the case of S30 extract of E. coli cells, a part or all ofthe following materials are added: Tris-acetate, DTT, NTPs (ATP, ACT,GTP (phosphoserine is added in addition to 20 kinds of natural aminoacids), polyethylene glycol (PEG), folic acid, cAMP, tRNA, ammoniumacetate, potassium acetate, potassium glutamate, magnesium acetate atsuitable concentration etc.

For expressing mutant PylRS in mammalian cells, the following may beperformed: DNA sequence of M. mazei-derived wild-type PylRS gene withHistidine-tag etc. at N terminus region thereof is amplified using PCR;this DNA sequence is integrated into an expression vector such ascommercially available pcDNA3.1 (Invitrogen) at NheI-BamHI site; and theconstructed plasmid is introduced into mammalian cells. Methods forintroducing a vector into cells may include, for example,electroporation, calcium phosphate method, lipofection and the like.

On the other hand, methods for expressing suppressor tRNA are notrestricted to particular ones, so suppressor tRNA may be expressed ineubacteria such as E. coli, or in eukaryotic cells such as mammaliancells according to methods known to a person skilled in the art. In thecase of expression in E. coli cells, for example, promoter sequence andterminator sequence are linked at 5′ terminus and 3′ terminus,respectively, of DNA encoding suppressor tRNA. Type-II promotertranscripting tRNA in eukaryotic cells is an internal promotercomprising 2 regions in tRNA cording sequence, consensus sequences ofwhich are known as box A and box B. Consensus sequence of box A isTRGCNNAGYNGG (SEQ ID NO:7) at positions 8-19, and consensus sequence ofbox B is GGTTCGANTCC (SEQ ID NO:8) at positions 52-62. Accordingly, in acase where, for example as is the case of suppressor tyrosine tRNA ofBacillus stearothermophilus, the cording sequence has box A and box B,suppressor tRNA can be expressed in animal cells without anymodification. In contrast, in a case where suppressor tRNA has nointernal promoter, the suppressor tRNA can be expressed using anexternal promoter in eukaryotic cells. For example, suppressor tRNA mayeffectively be expressed in animal cells by binding tRNA nucleic acidsequence or promoter sequence of Ul or U6 snRNA gene of eukaryote tosuppressor tRNA gene at 5′ terminus thereof. In further differentembodiments, suppressor tRNA may be coexpressed together with T7 RNApolymerase in animal cells by linking T7 phage-derived T7 promoter.

Further, the present invention provides a kit for synthesizing Z-Lysderivative-incorporated protein comprising (a) cell extract as mentionedabove, (b) a non-natural amino acid comprisingN^(ε)-benzyloxycarbonyl-lysine derivative, (c) the mutant PylRS of thepresent invention; and (d) a suppressor tRNA capable of binding to Z-Lysderivative in the presence of the mutant PylRS.

The “non-natural amino acid” as mentioned at (b) may be a mixture with20 kinds of natural amino acids. These components may be aliquoted forusability and be delivered as a kit for synthesizing Z-Lysderivative-incorporated protein. These products may be preserved infrozen or dried form, and marketed as a kit accommodating them in acontainer suitable for preservation and delivery. Instructions andvector DNA etc. may be enclosed in the kit.

EXAMPLE 1 Preparation and Crystallization of Sample

L-pyrrolysine:N⁶-[(2R,3R)-3-methyl-3,4-dihydro-2H-pyrrole-2-ylcarbonyl]-L-lysine (seeFIG. 1A) was chemically synthesized and its chemical structure wasconfirmed using H-NMR. Various derivatives of L-lysine were purchasedfrom Bachem AG (Switzerland). M. mazei-derived tRNA^(Pyl) wassynthesized by in vitro transcription and purified using RESOURCE Qcolumn chromatography (Amersham Biosciences Inc.).

The full length PylRS derived from M. mazei is a protein of molecularweight 51 kDa which consists of 454 amino acid residues. The geneencoding this full length PylRS was amplified using the followingprimers from genomic DNA of M. mazei JCM9314 strain (RIKEN BioResourceCenter) and cloned into a vector plasmid pET28c (Novagen Inc.) atNdeI-SacI site. This vector was introduced into E. coli cells to expressa protein, at the N terminus of which was linked pET28-derived His-tagcording region (MGSSHHHHHHSSGLVPRGSH) (SEQ ID NO:4).

N-terminal primer: (SEQ ID NO: 5)5′-AGGGGTAACCATATGGATAAAAAACCACTAAACAC-3′ C-terminal primer:(SEQ ID NO: 6) 5′-ACATGGTCCAGAGCTCTTACAGGTTGGTAGAAATCCCGTT-3′

On the other hand, although the full length PylRS was expressed in E.coli cells and its crystal was prepared, no crystal suitable for X-raystructural analysis was obtained. Accordingly, PylRS of which the 184amino acids from the N terminus were truncated (hereinafter referred toas “PylRS (c270)”; see FIG. 1B) was produced. At the N terminus of thePylRS (c270) protein was linked 6 repeats of Histidine-tag to produce afusion protein, which was expressed in E. coli BL21 (DE3) CodonPlus-RILstrain (Stratagene Inc.). According to the method disclosed in theabove-mentioned Non-Patent Document 3, the native PylRS (c270) proteinand a selenomethionine-labeled PylRS (c270) protein were purified andcrystallized. In order to obtain better crystal, crystallization wasconducted under slightly altered conditions, as follows: Cocrystal ofPylRS (c270) was obtained at ca. 20 degrees Celsius within 3 minutes in50 mM sodium cacodylate (pH 7.0) containing 5% PEG4000 (or PEG3350) and5 mM of MgCl₂ in the presence of 5 mM of pyrrolysine (or 3.45 mM ofBoc-Lys) and 5 mM of AMPPNP.

[Collection of Data]

According to the method disclosed in the above-mentioned Non-PatentDocument 3, collection of data for X-ray crystal structural analysis wasperformed. Using Beamline BL41XU in SPring-8, 1.8 angstrom data set froma crystal complex of PylRS(c270)/pyrrolysine/AMPPNP and 1.79 angstromdata set from a crystal complex of PylRS(c270)/Boc-Lys/AMPPNP werecollected.

[Structural Analysis]

MAD method was used to determine phase. Using SnB, 5 of 7 seleniumsubstitution sites were localized to calculate initial phase usingSOLVE. The initial phase was improved with density modification usingRESOLVE. A partial model was constructed automatically by RESOLVE, andthe remainder was constructed with Program 0 mainly and refined by CNS.Quality of conformational structural model was analyzed using PROCHECH.

[Aminoacylation Assay]

Mutagenesis of wild-type PylRS was performed using QuikChangeMutagenesis Kits (Stratagene Inc.). The full length PylRS mutant wasoverexpressed in E. coli cells, and then purified using HisTrap column(Amersham Biosciences Inc.). Aminoacylation reaction was performed atca. 37 degrees Celsius for 1 h. The reaction solution for aminoacylationcomprises 2.83 μM of purified PylRS derived from M. mazei (or 9 μM ofPylRS (c270)), 10 mM of MgCl₂, 2 mM of ATP, 4 mM of DTT, 2.11 μM oftranscript of M. mazei-derived tRNA^(Pyl), and adequate amount ofconcentrated solution of a variety of amino acids dissolved in 100 mM ofHEPES buffer (pH 7.2). Acid-urea polyacrylamide gel electrophoresis wasused to analyze whether tRNA had been aminoacylated or not.

[Entire Structure]

The PylRS of M. mazei consists of 454 amino acid residues and has highhomology with PylRS of M. barkeri (74% identity). The PylRS is mainlymade up of 2 domains. The C-terminal domain having approximately 250amino acid residues is of sequence homology with Class-II aminoacyl-tRNAsynthetase, whereas the N-terminal domain having approximately 140 aminoacid residues is unique (see FIG. 1B). The PylRS(c270) corresponding toan aminoacyl-tRNA synthetase-like domain may esterify tRNA^(Pyl) withpyrrolysine (see FIG. 1C). For crystal growth of this PylRS(c270), ATPanalogue needs to be added. In this regard, it is considered that ATPbinds tightly to PylRS (c270) to stabilize the structure thereof.

First, structure of AMPPNP-bound PylRS (c270) was determined bymulti-wavelength anomalous dispersion method (MAD method) usingselenomethionine-substituted one. The conformational structure thereofhad the distinctive feature of Class-II aaRS including lysyl-tRNAsynthetase (LysRS). In the PylRS (c270) structure, the residues atpositions 195-237 from N-terminus formed two α-helices (α1 and α2), andthe residues at positions 241-432 constituted a catalytic domain (seeFIG. 1D). The catalytic domain had an extended seven anti-parallelbeta-sheets (β1, β5, β6, β7, β8, β9, and β10) and an α-helix surroundingthem, and showed a characteristic topology of the class-II aaRSs.

FIG. 2 shows sequence alignments based on the conformations between M.mazei PylRS(c270), and other PylRS and LysRS. The sequences were alignedusing the program CLUSTAL W, and partially optimized manually. Highlyconserved amino acid residues between PylRS and LysRS were surroundedwith square frames. The secondary structures were schematicallyrepresented at the upper side of the aligned sequences. The amino acidsubstitution sites of tyrosine residue at position 306 and tyrosineresidue at position 384 relating to the present invention were indicatedwith arrows. The numerals at the upper side of the aligned sequencesrepresent the positions of amino acid residues of M. mazei PylRS (c270),and the numerals at the lower side of the aligned sequences representthose of E. coli LysRS. MmPylRSc represents Methanosarcina mazei PylRS(c270); MbPylRS represents Methanosarcina barkeri PylRS (AAL40867);MaPylRS represents Methanosarcina acetivoran PylRS (AAM03608); MtPylRSrepresents Methanosarcina thermophile PylRS; DhPylRSc representsDesulfitobacterium hafniense PylRS (AAU93507); EcLysU represents E. coliLysRS (AAA97029); MmLysRS represents Methanosarcina mazei Class-II LysRS(AAK29404); and HsLysRS represents human cytoplasmic LysRS (AAH04132).

[Recognition of Pyrrolysine and ATP]

Next, from the crystal structure of PylRS(c270) complexed withpyrrolysine and AMPPNP, it was found that the amino acid-binding site ofthe PylRS was much larger than that of the normal aminoacyl-tRNAsynthetase. The pyrrolysine molecule was bound on the surface of 7antiparallel β-sheets distinctive of the Class-II aminoacyl-tRNAsynthetase. Bulky 4-methyl-pyrroline ring is accommodated in a tunnel,which is mainly formed by hydrophobic residues, including Ala-302,Leu-305, Tyr306, Leu309, Cys348, Val-401, Leu-407, Ile-413, and Trp417(see FIGS. 3A and 3C). The amide moiety of the Asn-346 side chain facesto an amino acid substrate and forms a hydrogen bond at a distance of2.82 angstrom with the side-chain carbonyl group of the pyrrolysine tofix the position thereof. In contrast, in a case where pyrrolysine is anaxial type stereoisomer, the distance between the amide moiety of theAsn-346 side chain and the side-chain carbonyl group of the pyrrolysinewas 2.81 angstrom (see FIGS. 3E and 3F). Further, the carbonyl group ofthe Asn-346 side chain binds indirectly to the alpha-amino group of thepyrrolysine with a hydrogen bond through a water molecule. The guanidiumgroup of Arg-330 highly conserved binds to the α-carbonyl group ofpyrrolysine with a hydrogen bond. There are no hydrogen bonds other thanthese 3 hydrogen bonds at Asn-346 and Arg-330. This amino acidrecognition mechanism of PylRS is very distinctive (see FIG. 3C). Theaminoacylation activities of the PylRS mutants comprising a substitutionat any one of amino acid residues which form the tunnel accommodatingthe pyrrolysine were determined, resulting in that the activities of the5 mutants, in which alanine was substituted correspondingly for leucineat position 305, tyrosine at position 306, asparagine at position 346,valine at position 401 and tryptophan at position 417 were decreaseddrastically (see FIG. 3B).

[Comparison Between the Active Sites of the PylRS and the LysRS]

The structure of the PylRS and its substrate binding mechanism werecompared with those of Escherichia coli LysRS. In the active site of E.coli LysRS, highly conserved residues (Glu-240, Arg-262, Glu-278,Tyr-280, Asn-424, Phe-426, and Glu-428) are involved in L-lysinerecognition (see FIG. 3D). In a case where these residues aremutagenized, Km value for L-lysine which is a substrate of LysRS isincreased drastically. On the contrary, Arg-262 is merely conserved inM. mazei PylRS(c270), and the other positions are occupied by smaller,uncharged amino acid residues (Ala-302, Asn-346, Cys348, Ser-399,Val-401, and Gly-403). By these amino acid substitutions, the aminoacid-binding site (tunnels) in PylRS is 8 to 9 angstrom deeper than thatof the L-lysine-binding pocket in LysRS (see FIG. 3A). As describedabove, only 3 hydrogen bonds are formed between pyrrolysine and PylRS(c270), whereas at least 7 hydrogen bonds are formed between L-Lys andLysRS. The small number of hydrogen bonds interacting with the lysinemoiety makes it difficult for PylRS to activate L-lysine as a substrate.Actually, PylRS activates tRNA^(Pyl) with pyrrolysine at a concentrationof 1 mM, whereas it cannot activate 20 kinds of normal amino acidsincluding lysine even at a concentration of 0.5 M. Intriguingly, inpyrrolysine recognition by PylRS, a moiety corresponding to the lysineside chain serves as a spacer between the main chain and themethyl-pyrroline carbonyl moiety. The deep hydrophobic tunnel and weakrecognition of the lysyl moiety are great differences between PylRS andLysRS in substrate recognition.

[Activation of Non-Natural Amino Acids by PylRS]

From the conformational structure of the substrate recognition site ofthe PylRS, it was surmised that PylRS could activate non-natural aminoacid other than pyrrolysine. Based upon this hypothesis, it was examinedwhether PylRS could activate 6 kinds of NE-lysine derivatives shown inFIG. 4A. The results were shown in FIG. 4B. In each lane, aminoacylationwas conducted in the presence of PylRS under the following condition(which is shown starting from the left column): no amino acid; 0.5 MLys; 100 mM Ac-Lys; 1 mM Boc-Lys; 1 mM Aloc-Lys; 10 mM Nic-Lys; 7 mMNma-Lys; 3.5 mM Z-Lys; 1 mM pyrrolysine; and control tRNA^(Pyl). Asdemonstrated in FIG. 4B, tert-butyloxycarbonyl-lysine (Boc-Lys) andallyloxycarbonyl-lysine (Aloc-Lys) were activated at a concentration of1 mM, as efficiently as pyrrolysine. Furthermore, it was found that thewild-type PylRS esterified tRNA^(Pyl) with NE-modified lysinederivatives, such as N^(ε)-acetyl-L-lysine (Ac-Lys),NE-nicotinoyl-L-lysine (Nic-Lys), N^(ε)-benzyloxycarbonyl-L-lysine(Z-Lys), N^(ε)-(N-methyl-anthraniloyl)-L-lysine (Nma-Lys) which was afluorescent amino acid, and the like. On the contrary, wild-type PylRScould not activate lysine derivatives which were N^(ε)-linkaged withmethyl, dimethyl, trimethyl, isopropyl, dansyl, o,p-dinitrophenyl,p-azidobenzoyl, biotinyl, 9-fluorenylmethoxycarbonyl, andp-toluenesulfonyl groups. Accordingly, it was found that PylRS couldrecognize N^(ε)-substituents having bulkiness at a certain range.

The aminoacylation activity of the PylRS mutants produced as mentionedabove were determined using Boc-Lys as a substrate, resulting in thatthe catalytic activities of the 5 mutants in which alanine wassubstituted correspondingly for leucine at position 305, tyrosine atposition 306, asparagine at position 346, valine at position 401 andtryptophan at position 417 were decreased drastically. Intriguingly, itwas found that one PylRS(c270) mutant (Y306A) esterified tRNA^(Pyl) withZ-Lys much more efficiently than the wild-type PylRS (see FIG. 5C). Itis considered that this mutation having the substitution of tyrosine atposition 306 by alanine generates a cavity suitable to accommodate thebenzyloxycarbonyl (Z) group at substrate-binding site of PylRS (FIGS. 5Aand 5B).

[Selection of the Boc-Lys-tRNA Synthetase]

From the results of aminoacylation assay in vitro, it was found thatalthough the wild-type PylRS aminoacylated lysine derivatives such asBoc-Lys, these derivatives could not efficiently be incorporated into aprotein in E. coli cells. Accordingly, the PylRS mutant (Y384F) capableof incorporating Boc-Lys into a protein in vivo efficiently was screenedby the following method.

The full length PylRS gene was expressed under the control of E. coliTyrRS promoter and terminator in plasmid pTK2-1. This plasmid pTK2-1 isa derivative of plasmid pACYC184 and expresses one copy of thetRNA^(Pyl) gene under the control of the kanamycin resistant gene andthe E. coli lpp promoter. The PylRS gene was mutagenized randomly at aratio of three to seven mutations per kb using the GeneMorph PCRmutagenesis kit (Stratagene), and was ligated with the original plasmidpTK2-1 to generate a PylRS library. The ligated vectors were transformedinto DH10B competent cells to yield a library of 6×10⁷ colony formingunits. The tRNA^(Pyl) gene was also expressed in E. coli DH10B cellsunder the control of the lpp promoter and the rrnC terminator in plasmidpTK2-1. The PylRS mutant library was first subjected to a positiveselection based on suppression of an amber stop codon located at anonessential position in the chloramphenicol acetyltransferase (CAT)gene. The cells transformed with the PylRS mutant library and thewild-type tRNA^(Pyl) gene were grown in media containing 1 mM Boc-Lys,and cells capable of surviving in the presence of various concentrationsof chloramphenicol were screened. Then the surviving cells were grown inthe presence of chloramphenicol and the absence of Boc-Lys. In theabsence of Boc-Lys, the cells expressing selected PylRS mutants survivedmerely at the concentration of less than 25 μg/ml of chloramphenicol,whereas in the presence of Boc-Lys, they survived at the concentrationof 150 μg/ml of chloramphenicol. Comparing with the CAT resistance of E.coli in the absence of PylRS (<13 μg/ml), these results demonstrate thatthe selected PylRS mutant (Y384F) aminoacylates Boc-Lys, and furtheraminoacylates any natural amino acids to some degree.

[Lysine Derivative-Dependent Amber Suppression in E. coli Cells.]

In order to confirm whether amber suppression (amber mutationsuppression) occurs in E. coli cells, the glutathione S-transferase(GST) gene whose tyrosine codon at the 25th from N terminus was mutatedto the amber codon (TAG) was cloned into a pET system plasmid. On theother hand, the wild-type and a variety of mutant PylRS genes, as wellas tRNA^(Pyl) genes were cloned into a pACYX system plasmid (see FIG.6). These two expression vectors were transformed to E. coli BL21 (DE3)to statically culture overnight on LB agar medium including kanamycinand ampicillin. Growing colonies were inoculated into LB liquid mediumincluding kanamycin and ampicillin in the presence or absence of lysinederivative, and cultured at ca. 37 degrees Celsius, followed by additionof IPTG such that its final concentration was equivalent to 1 mM whenthe absorbance of the medium reached to 0.6. Incubation was conductedovernight to induce expression before E. coli cells were harvested todetect expressed GST using SDS-PAGE. As a result, it was observed that28-kDa GST protein was expressed in a case where the mutant PylRS(Y384F) and tRNA^(Pyl) were expressed in the presence of 4 mM of Boc-Lysand in a case where they were expressed in the presence of 4 mM ofAloc-Lys (see FIG. 7). It was also observed that the full length GSTprotein was produced in a case where double mutant PylRS (Y384F/Y306A)and tRNA^(Pyl) were expressed in the presence of 5 mM Z-Lys (see FIG.8). E. coli cells recovered from 10 ml of the culture medium weresupplied with 1 ml of buffer A (potassium phosphate (pH 7.4), 0.15M ofNaCl and 10 mM of (3-mercaptoethanol) to be subjected to sonication andcentrifugation. The resulting supernatant was supplied with 200 μl ofglutathione affinity column (GSTrap, Amersham Biosciences Inc.), andstirred at ca. 4 degrees Celsius for 1 h, followed by washing 3 timeswith buffer A to elute GST protein with buffer A containing 20 mM ofglutathione. The thus purified GST protein was yielded 1 to 2 mg ofproteins per liter of medium (see FIG. 9). The purified GST protein wasdegraded with trypsin to analyze with MALDI-TOF mass spectrometry.Detection peaks corresponding to peptides NSXSPIGYWK (X representsBoc-Lys, Aloc-Lys or Z-Lys) (SEQ ID NO: 18) which were generated withtrypsin digestion were m/z=1392.74, 1376.79 and 1426.70 Da, which agreedwell with the theoretical values, and were by 65.02, 49.07 and 98.98 Da,respectively, greater than those of the wild-type tryptic peptideNSYSPILGYWK (SEQ ID NO: 17) (m/z=1327.72 Da) (see FIG. 10). The sequenceinformation from the mass spectrums represented in FIG. 10 demonstratesthat these non-natural amino acids were site-specifically incorporatedinto a GST protein.

[Docking Model of PylRS(c270) with tRNA]

It is notable that the PylRS(c270) maintains the aminoacylation activityof tRNA (see FIG. 1C). This finding indicates that tRNA^(Pyl) may bindto the PylRS of which N-terminal domain is deleted. The catalyticactivity site of the PylRS (c270) was superposed onto the tertiarystructure of the E. coli aspartic acid-tRNA synthetase complexed withtRNA^(Asp) to make a binding model in which tRNA^(Asp) was replaced withyeast tRNA^(Phe). According to this model, the PylRS (c270) contactswith the acceptor stem and the D arm of tRNA. The α1 and α2 helices wereadjacent to the D arm of one tRNA protomer. No interaction of PylRS(c270) with the T arm and the anticodon arm was observed. The structureof tRNA^(Pyl) has features significantly different from those of normaltRNAPhe, for example, a small D loop consisting only of 5 bases, asshown in FIG. 11A. The full length PylRS of M. mazei may also contactwith the T arm of tRNA^(Pyl), since the N-terminal helix of thePylRS(c270) protrudes toward the T arm. In addition, mutants in whichanticodon sequences of tRNA^(Pyl) were changed to different sequenceswere produced, none of which affected the enzymatic activity of PylRS.Thus, it has been found that PylRS does not interact with the anticodonloop of tRNA and requires almost no anticodon recognition (see FIG.11B).

EXAMPLE 2 Screening of Z-Lys Specific PylRS Mutant

On the basis of the conformational structure of PylRS (c270) complexedwith Boc-Lys and AMPPNP, Z-Lys-specific mutant PylRS was screened by thefollowing method. Of the conformational structure of this complex, theamino acid residue of PylRS localized at position adjacent to the sidechain of Boc-Lys was selected to perform saturation mutagenesis. Forrecognizing the large Z-Lys group, the terminal portion in the aminoacid recognition pocket of PylRS must enlarge and widen. In the complexstructure of PylRS and Boc-Lys, Tyr306, Leu309, Cys348 and Trp417constitute the terminal portion of the pocket. However, since thesubstitution of Trp417 of PylRS by a different amino acid causes loss ofthe enzymatic activity, a library of mutant enzymes in which codons ofthe other 3 amino acid residues were replaced with NNK (wherein Nrepresents any of 4 kinds of bases and K represents G or T) was produced(containing 2.3×10⁶ of independent transformants).

Concretely, the R61K, G131E and Y384F mutant PylRS genes with increasedaminoacylation activity against Boc-Lys were cloned under control ofglnS promoter in the plasmid pBRQ1 comprising pBR322 replication originand kanamycin resistant gene. DNA fragments of these PylRS genes whosecodon sequences at positions 306, 309 and 348 were randomly replacedwith NNK (wherein N represents any of 4 kinds of bases and K representsG or T) were synthesized and amplified by PCR. These fragments wereconstructed by overlap PCR method to insert into a region downstream ofglnS promoter in plasmid pBRQ1. These plasmids were introduced into E.coli DH10B carrying a plasmid which contains tRNA^(Pyl) gene undercontrol of CAT gene (AM112) having amber mutation and lpp promoter. Aspositive selection, the resulting transformant was selected on LB platecontaining 50 ug/ml of chloramphenicol and 1 mM of Z-Lys, and plasmidDNA was extracted and purified with agarose gel electrophoresis.Subsequently, the resulting plasmid DNA was introduced into E. coliDH10B carrying a pACYC184-derived plasmid comprising DNA which had ambercodons at positions 2, 44 and 65 in coding region of the barnase gene,which was a bacterial toxin, and were controlled by araC promoter. Asnegative selection, these cells were incubated on LB plates containing0.02% arabinose. The positive selection was repeated 3 times and thenegative selection was repeated twice.

As a result, finally 5 mutants were obtained by the positive selectionusing 75 μg/ml of chloramphenicol. It was observed that of these 5mutants, a cell which had an enzyme (hereinafter referred to as Z-LysRS)having double amino acid substitution of L309A and C348V expressedamber-suppressed GST most abundantly (6.9 mg/L medium in M9 GMML mediumcontaining 1 mM of Z-Lys) but showed little expression under thecondition of non addition of Z-Lys (see FIG. 13).

FIG. 13 shows results obtained from researches of expressions of thefull length GST amber-suppressed such that the mutant PylRS (Y306A)obtained in Example 1 and the Z-LysRS obtained in Example 2 were usedand 2 kinds of non-natural amino acid Z-Lys(s) or 2-chloro-Z-Lys wasadded. The upper part and lower part of FIG. 13 show results obtainedfrom 12% SDS-PAGE separation and CBB staining of crude extract from E.coli cells and purified GST solution, respectively. The yields in eachcondition (level (mg) of GST expression per 1 L of M9 GMML medium) weredetermined according to Bradford method (using BioRad Protein AssayKit), the results of which were shown in blank between two gelspositioned on the upper and lower sides. In FIG. 13, N.D. represents“undetectable”.

The purified GST protein was subjected to trypsin digestion and thenanalyzed with MALDI-TOF mass spectrometry, resulting in that a peptidepeak corresponding to NSXSPIGYWK (SEQ ID NO: 18) (wherein X representsZ-Lys residue, m/z=1426.75 Da) was merely detected and none of peaks ofpeptides incorporated with other amino acids were detected. Accordingly,it was found that the mutant enzymes Z-LysRS (L309A, C348V) obtained inExample 2 were specific to Z-Lys. Further, it is considered thatbecause, as shown in FIG. 13, Z-LysRS has higher incorporationefficiency of Z-Lys than Y306A whereas the former has lower amount of2-chloro-derivative as a substrate than the latter, Z-LysRS has higherspecificity to Z-Lys than Y306A.

EXAMPLE 3 Incorporation of N^(ε)-Ortho-Azide-Benzyloxycarbonyl-Lysine(AzZLys) into GST Protein in E. coli Cells and Modification ReactionThereof

The same plasmid pTK2-1 as Example 1 was used for expressing PylRSmutant with double amino acid substitutions of Y306A and Y384F andtRNA^(Pyl) in E. coli cells. Incorporation of a lysine derivative intoGST having amber codon at 25th from its N-terminus using this plasmidwas performed according to the same method as Example 1. Moreover,specific incorporation of AzZLys [purchased from Shinsei ChemicalCompany Ltd. (Osaka)] into the amber site in GST using the same plasmidwas also performed according to the same method as Example 1.Subsequently, crude extract obtained from E. coli cells in which the GSTamber gene was expressed was separated with SDS-PAGE and stained. As aresult, expression of the full length GST was detected merely in thecase of the presence of 1 mM AzZLys (+) (in FIG. 14, the position of thedetected band is indicated with an arrow of GST). Furthermore,purification of GST was performed with the same method as Example 1.

A conjugate of fluorophore and triarylphosphine, and the purified fulllength GST were linked by Staudinger-Bertozzi reaction. As a conjugate,the conjugate with FITC (hereinafter referred to as FITC-PP3) (purchasedfrom Shinsei Chemical Company Ltd.) was used. FIG. 15 shows the chemicalstructure of FITC-PP3. Linkage reaction was performed under two types ofreactive conditions, i.e., at ca. 37 degrees Celsius for 1 hour (lhr)and at ca. 4 degrees Celsius overnight (O/N). Subsequently, these GSTwere separated by SDS-PAGE to detect fluorescence with UV light. As aresult, fluorescence-modified GST was detected merely in the case of thereactive condition at ca. 37 degrees Celsius for 1 hour (in FIG. 16, theposition of the detected band is indicated with an arrow of GST). As tothe Staudinger-Bertozzi reaction, see the above-mentioned Non-PatentDocuments 5, 6, etc. This result suggests that it is possible tospecifically incorporate AzZLys into a desired site in E. coli by usingPylRS (Y306A, Y384F) mutant, and that it is possible to incorporate anymodification group containing fluorophore into (any) protein [GSTprotein] by reacting the incorporated AzZLys with phosphine.

[Incorporation of AzZLys into Grb2 Protein in Animal Cell andFluorescent Modification Reaction]

For expressing PylRS (Y306A, Y384F) mutant and tRNA^(P1) in HEK c-18cell, the system disclosed in the above-mentioned Non-Patent Document 7was used. Likewise, the mutant gene into which the amber codon wasincorporated at the cording region of lac Z gene and GRB2 gene, and theexpression system thereof, as disclosed in the above-mentionedNon-Patent Document 7, were used.

First, in the animal cells, optimal concentration of AzLys forsite-specific incorporation of AzLys into the protein was determined. Inmedia containing 0, 0.01, 0.025, 0.05, 0.1, 0.25 and 0.5 mM of AzZLys,LacZ protein was expressed from the lacZ amber gene to determine thelevel of expression (relative value) of LacZ with coloring reaction byLacZ. As a result, it was found that AzZLys was most efficientlyincorporated into the amber site of lacZ in the case of AzZLys beingadded at the concentration of 0.05 mM (see FIG. 17). In FIG. 17, WTrepresents the level of expression (relative value) of wild-type (WT)lacZ without any amber codon in the coding region. In comparison to theresult of WT, it is apparent that suppression efficiency in the case ofthe concentration of AzZLys being 0.05 mM is equal to approximately 30%of WT.

Fluorescein phosphine•conjugate (FITC-PP3) was added to crude extractfrom the animal cells in which the GRB2 amber gene was expressed,whereby a Grb2 protein was labeled with fluorescence. Subsequently,separation with SDS-PAGE was performed to detect fluorescence withfluorescence detector (see FIG. 18, at lanes 1 to 3). In FIG. 18, aaRSrepresents the presence or absence of ZLys expression (“+” representsthe presence of the expression), Grb2 represents the presence or absenceof GRB2 amber gene expression (“Am” represents the presence of theexpression), tRNA represents the presence or absence of tRNA^(Pyl)expression (“+” represents the presence of the expression); and a.a.represents the presence or absence of AzZLys addition (“+” representsaddition). As is evident from FIG. 18, a Grb2 protein labeled withfluorescence was detected merely in the case of aaRS (+), Grb2 (Am),tRNA (+) and a.a. (+) (at lane 3) (wherein the position of the detectedband is indicated with an arrow of GST). Incidentally, lane 1 representsthe result of WT in the case of the GRB2 gene being used. As is apparentfrom FIG. 18, no fluorescence labeling bands were detected in lane 1. Asa control, para-azide-phenylalanine (hereinafter referred to as AzF) wasincorporated into the same site of the Grb2 protein. In order toincorporate AzF into the amber site in animal cells using AzF-specificenzyme (AzFRS), the system disclosed in the above-mentioned Non-PatentDocument 8 was used. As is evident from FIG. 18, Grb2 was modified withfluorescence also in the case of AzFRS being used (at lane 5; theposition of the detected band is indicated with an arrow of Grb2), andalso AzFRS was modified with fluorescence concurrently (at lanes 5 and6, the positions of the detected bands are indicated with an arrow ofAzFRS). This result demonstrates that the distinction between Grb2 andAzFRS cannot be made only by detection of fluorescence, and thus suchmethod is inconvenient.

The above-mentioned results demonstrate that it is possible tospecifically incorporate AzZLys into a desired site in animal cells byusing PylRS (Y306A, Y384F) mutant and that it is possible to incorporateany arbitrary modification group comprising fluorophore into (anyarbitrary) protein [GST protein] by reacting the incorporated AzZLyswith phosphine. The above-mentioned results further demonstrate that thesystem of the present invention used in these Examples is superior inselectivity of modification to conventional systems for incorporatingAzF into a protein using AzFRS.

The mutant PylRS of the present invention allows a site-specificincorporation of a non-natural amino acid such as a Z-Lys derivativeinto a protein, which could not be conducted so far, and thus is usefulfor synthesizing novel alloproteins. By providing those means, thepresent invention promotes understanding of complex biological phenomenavia analysis of the structure and function of proteins, and thus isindustrially applicable in the fields of pharmaceuticals and lifescience.

It should be noted that changes and modifications of the embodiments orExamples may be done within the entire disclosure (inclusive of theclaims) of the present invention and on the basis of the basic technicalspirits thereof. Also, it should be noted that a variety of combinationsor selections of various elements disclosed may be made within the scopeof the claims of the present invention.

In the present invention, there are further possible modes as follows.

Mode 1 is as set forth in the first aspect.Mode 2: The mutant pyrrolysyl-tRNA synthetase of Mode 1 may furthercomprise amino acid substitution of phenylalanine or histidine fortyrosine at position 384.Mode 3: In the mutant pyrrolysyl-tRNA synthetase of Mode 2, the aminoacid substitution may comprise double substitution in which alanine issubstituted for tyrosine at position 306 and phenylalanine issubstituted for tyrosine at position 384.Mode 4: In the mutant pyrrolysyl-tRNA synthetase of Mode 2, the aminoacid substitution may comprise double substitution in which alanine issubstituted for leucine at position 309 and phenylalanine is substitutedfor tyrosine at position 384.Mode 5: In the mutant pyrrolysyl-tRNA synthetase of Mode 2, the aminoacid substitution may comprise triple substitution in which alanine issubstituted for leucine at position 309, valine is substituted forcysteine at position 348, and phenylalanine is substituted for tyrosineat position 384.Mode 6: The mutant pyrrolysyl-tRNA synthetase of any one of Modes 1 to5, whose amino acid sequence may comprise one or several amino aciddeletions, substitutions, or additions at positions other than atpositions 306, 309, 348 and 384, and which is capable of aminoacylatingN^(ε)-benzyloxycarbonyl-lysine.Mode 7: A mutant pyrrolysyl-tRNA synthetase, obtained from a wild-typepyrrolysyl-tRNA synthetase, which is Methanosarcina-derivedpyrrolysyl-tRNA synthetase that is a homolog of the amino acid sequenceset forth in SEQ ID NO:2, so substituted that when the amino acidsequence of the homolog is aligned with the amino acid sequence setforth in SEQ ID NO:2, the homolog has substitution of alanine fortyrosine corresponding to position 306 of the amino acid sequence setforth in SEQ ID NO:2 and/or substitution of phenylalanine for tyrosinecorresponding to position 384 thereof.Mode 8: An isolated DNA encoding the mutant pyrrolysyl-tRNA synthetaseof any one of Modes 1 to 7, according to the second aspect.Mode 9: In an expression vector which, when it is introduced into a hostcell, is capable of producing the mutant pyrrolysyl-tRNA synthetase ofany one of Modes 1 to 7 in host cell, the expression vector may comprisethe DNA of Mode 8 which is functionally bound to an expression controlsequence in the host cell.Mode 10: Eubacterium transformed with the expression vector of Mode 9.Mode 11: Escherichia coli transformed with the expression vector of Mode9.Mode 12: Mammalian culture cell transformed with the expression vectorof Mode 9.Mode 13: A method of producing a non-natural amino acid-incorporatedprotein according to the third aspect.Mode 14: In the method of Mode 13, the aminoacyl-tRNA synthetase may bethe mutant pyrrolysyl-tRNA synthetase of any one of Modes 1 to 5.Mode 15: In the method of Mode 13 or 14, theN^(ε)-benzyloxycarbonyl-lysine derivative may be:

-   N^(ε)-ortho-iodo-benzyloxycarbonyl-lysine;-   benzyloxycarbonyl-aminoethyl-selenocysteine;-   N^(ε)-ortho-ethinyl-benzyloxycarbonyl-lysine;-   N^(ε)-ortho-azide-benzyloxycarbonyl-lysine; or-   N^(ε)-ortho-diaziryl-benzyloxycarbonyl-lysine.    Mode 16: A kit for synthesizing non-natural amino acid-incorporated    protein according to the fourth aspect.

What is claimed is:
 1. A mutant pyrrolysyl-tRNA synthetase comprisingsubstitution of at least one amino acid residue selected from tyrosineat position 306, leucine at position 309, and cysteine at position 348,which constitute a pyrrolysine-binding site, in the amino acid sequenceof the pyrrolysyl-tRNA synthetase set forth in SEQ ID NO:2, wherein saidsubstitution of the amino acid residue comprises: substitution ofglycine or alanine for tyrosine at position 306, substitution of glycineor alanine for leucine at position 309, and/or substitution of valine,serine or alanine for cysteine at position 348, wherein said mutantpyrrolysyl-tRNA synthetase aminoacylates a pyrrolysine tRNA withN^(ε)-benzyloxycarbonyl-lysine derivative more efficiently than the wildtype pyrrolysyl-tRNA synthetase having the amino acid sequence set forthin SEQ ID NO:2.
 2. The mutant pyrrolysyl-tRNA synthetase of claim 1,further comprising amino acid substitution of phenylalanine or histidinefor tyrosine at position
 384. 3. The mutant pyrrolysyl-tRNA synthetaseof claim 2, wherein said amino acid substitution comprises doublesubstitution in which alanine is substituted for tyrosine at position306 and phenylalanine is substituted for tyrosine at position
 384. 4.The mutant pyrrolysyl-tRNA synthetase of claim 2, wherein said aminoacid substitution comprises double substitution in which alanine issubstituted for leucine at position 309 and phenylalanine is substitutedfor tyrosine at position
 384. 5. The mutant pyrrolysyl-tRNA synthetaseof claim 2, wherein said amino acid substitution comprises triplesubstitution in which alanine is substituted for leucine at position309, valine is substituted for cysteine at position 348, andphenylalanine is substituted for tyrosine at position
 384. 6. The mutantpyrrolysyl-tRNA synthetase of claim 1, whose amino acid sequencecomprises one or several amino acid deletions, substitutions, oradditions at positions other than at positions 306, 309, 348 and 384,and which is capable of aminoacylating N^(ε)-benzyloxycarbonyl-lysinederivative.
 7. A mutant pyrrolysyl-tRNA synthetase, obtained from awild-type pyrrolysyl-tRNA synthetase, which is Methanosarcina-derivedpyrrolysyl-tRNA synthetase that is a homolog of the amino acid sequenceset forth in SEQ ID NO:2, so substituted that when the amino acidsequence of said homolog is aligned with the amino acid sequence setforth in SEQ ID NO:2, the homolog has substitution of alanine fortyrosine corresponding to position 306 of the amino acid sequence setforth in SEQ ID NO:2 and/or substitution of phenylalanine for tyrosinecorresponding to position 384 thereof; and the mutant pyrrolysyl-tRNAsynthetase aminoacylates a pyrrolysine tRNA withN^(ε)-benzyloxycarbonyl-lysine derivative.
 8. An isolated DNA encodingthe mutant pyrrolysyl-tRNA synthetase of claim
 1. 9. An expressionvector which, when it is introduced into a host cell, is capable ofproducing the mutant pyrrolysyl-tRNA synthetase of claim 1 in host cell,wherein the expression vector comprises an isolated DNA encoding of themutant pyrrolysyl-tRNA synthetase of claim 1 which is functionally boundto an expression control sequence in said host cell.
 10. Eubacteriumtransformed with the expression vector of claim
 9. 11. Escherichia colitransformed with the expression vector of claim
 9. 12. Mammalian culturecell transformed with the expression vector of claim
 9. 13. A method ofproducing a non-natural amino acid-incorporated protein wherein thefollowing (a) to (c) are expressed in a cell or cell extract in thepresence of an N^(ε)-benzyloxycarbonyl-lysine derivative: (a) anaminoacyl-tRNA synthetase capable of activating theN^(ε)-benzyloxycarbonyl-lysine derivative; (b) a suppressor tRNA capableof binding to the N^(ε)-benzyloxycarbonyl-lysine derivative in thepresence of said aminoacyl-tRNA synthetase, and (c) a gene encoding adesired protein that has nonsense mutation or frameshift mutation at adesired position.
 14. The method of claim 13, wherein saidaminoacyl-tRNA synthetase is the mutant pyrrolysyl-tRNA synthetase ofclaim
 1. 15. The method of claim 13, wherein saidN^(ε)-benzyloxycarbonyl-lysine derivative comprises:N^(ε)-ortho-iodo-benzyloxycarbonyl-lysine;benzyloxycarbonyl-aminoethyl-selenocysteine;N^(ε)-ortho-ethinyl-benzyloxycarbonyl-lysine;N^(ε)-ortho-azide-benzyloxycarbonyl-lysine; orN^(ε)-ortho-diaziryl-benzyloxycarbonyl-lysine.
 16. A kit forsynthesizing non-natural amino acid-incorporated protein comprising: (a)cell extract; (b) a non-natural amino acid comprisingN^(ε)-benzyloxycarbonyl-lysine derivative; (c) the mutantpyrrolysyl-tRNA synthetase of claim 1; and (d) a suppressor tRNA capableof binding to an N^(ε)-benzyloxycarbonyl-lysine derivative in thepresence of said mutant pyrrolysyl-tRNA synthetase.
 17. An isolated DNAencoding the mutant pyrrolysyl-tRNA synthetase of claim
 2. 18. Anexpression vector which, when it is introduced into a host cell, iscapable of producing the mutant pyrrolysyl-tRNA synthetase of claim 2 inhost cell, wherein the expression vector comprises an isolated DNAencoding of the mutant pyrrolysyl-tRNA synthetase of claim 2 which isfunctionally bound to an expression control sequence in said host cell.19. Escherichia coli transformed with the expression vector of claim 18.20. Mammalian culture cell transformed with the expression vector ofclaim 18.